Hemophilia A [hemofilie A]

topical
688
Terms

autozomální hemofilie A
chybění faktoru VIII
deficit faktoru VIII
deficit koagulačního faktoru VIII
hemofilie
nedostatek faktoru VIII
nedostatek koagulačního faktoru VIII
vrozený deficit faktoru VIII

 

Autosomal Hemophilia A
Classic Hemophilia
Deficiency, Factor VIII
Factor 8 Deficiency, Congenital
Factor VIII Deficiency
Factor VIII Deficiency, Congenital
Haemophilia
Hemophilia
Hemophilia A, Congenital
Hemophilia, Classic

Persistent link   https://www.medvik.cz/link/D006467
Definition

The classic hemophilia resulting from a deficiency of factor VIII. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.

DUI
D006467 MeSH Browser
CUI
M0010149
History note
1999(1966)
Public note
1999; see HEMOPHILIA 1966-1998; for HEMOPHILIA A see HEMOPHILIA 1993-1998

C Diseases
C15.378.100.100.037 Activated Protein C Resistance 105
C15.378.100.100.056 Afibrinogenemia 39
C15.378.100.100.075 Antithrombin III Deficiency 24
C15.378.100.100.080 Bernard-Soulier Syndrome 9
C15.378.100.100.300 Factor V Deficiency 7
C15.378.100.100.310 Factor VII Deficiency 6
C15.378.100.100.320 Factor X Deficiency 2
C15.378.100.100.325 Factor XI Deficiency 12
C15.378.100.100.330 Factor XII Deficiency 8
C15.378.100.100.335 Factor XIII Deficiency 4
C15.378.100.100.500 Hemophilia A 688
C15.378.100.100.510 Hemophilia B 214
C15.378.100.100.515 Hermanski-Pudlak Syndrome 7
C15.378.100.100.550 Hypoprothrombinemias 4
C15.378.100.100.690 Protein C Deficiency 31
C15.378.100.100.820 Thrombasthenia 7
C15.378.100.100.900 von Willebrand Diseases 103
C15.378.100.100.970 Wiskott-Aldrich Syndrome 20
C15.378.100.141.036 Activated Protein C Resistance 105
C15.378.100.141.072 Afibrinogenemia 39
C15.378.100.141.300 Factor V Deficiency 7
C15.378.100.141.310 Factor VII Deficiency 6
C15.378.100.141.320 Factor X Deficiency 2
C15.378.100.141.325 Factor XI Deficiency 12
C15.378.100.141.330 Factor XII Deficiency 8
C15.378.100.141.335 Factor XIII Deficiency 4
C15.378.100.141.500 Hemophilia A 688
C15.378.100.141.510 Hemophilia B 214
C15.378.100.141.550 Hypoprothrombinemias 4
C15.378.100.141.900 von Willebrand Diseases 103
C15.378.463.067 Afibrinogenemia 39
C15.378.463.080 Bernard-Soulier Syndrome 9
C15.378.463.300 Factor V Deficiency 7
C15.378.463.310 Factor VII Deficiency 6
C15.378.463.320 Factor X Deficiency 2
C15.378.463.325 Factor XI Deficiency 12
C15.378.463.330 Factor XII Deficiency 8
C15.378.463.335 Factor XIII Deficiency 4
C15.378.463.500 Hemophilia A 688
C15.378.463.510 Hemophilia B 214
C15.378.463.515 Hemostatic Disorders 49
C15.378.463.550 Hypoprothrombinemias 4
C15.378.463.810 Thrombasthenia 7
C15.378.463.825 Thrombocythemia, Essential 93
C15.378.463.841 Vitamin K Deficiency 42
C15.378.463.920 von Willebrand Diseases 103
C15.378.463.960 Wiskott-Aldrich Syndrome 20
C16.320.099.056 Afibrinogenemia 39
C16.320.099.080 Bernard-Soulier Syndrome 9
C16.320.099.300 Factor V Deficiency 7
C16.320.099.310 Factor VII Deficiency 6
C16.320.099.320 Factor X Deficiency 2
C16.320.099.325 Factor XI Deficiency 12
C16.320.099.330 Factor XII Deficiency 8
C16.320.099.335 Factor XIII Deficiency 4
C16.320.099.417 Gray Platelet Syndrome 1
C16.320.099.500 Hemophilia A 688
C16.320.099.510 Hemophilia B 214
C16.320.099.515 Hermanski-Pudlak Syndrome 7
C16.320.099.550 Hypoprothrombinemias 4
C16.320.099.690 Protein C Deficiency 31
C16.320.099.820 Thrombasthenia 7
C16.320.099.920 von Willebrand Diseases 103
C16.320.099.970 Wiskott-Aldrich Syndrome 20